An Observational Study Called FINE-REAL Korea to Learn More About the Use of the Drug Finerenone in People With Chronic Kidney Disease and Type 2 Diabetes in a Routine Medical Care Setting in South Korea

NCT07232537 | Recruiting

• 1 other identifier: 23104
• Study Type: observational
• Target: 500
• Locations: 1 country
• Sites: 1

Brief Summary

This is an observational study in which data from people with chronic kidney disease (CKD) and type 2 diabetes (T2D) who will be receiving finerenone are collected and studied. Chronic kidney disease is a long-term condition where the kidneys gradually lose their ability to filter waste and extra water from the blood. Type 2 diabetes occurs when the body does not produce enough insulin or does not use it effectively, leading to high blood sugar levels that can harm the kidneys. As a result, CKD can develop as a complication of T2D. The study drug, finerenone, is already approved for doctors to prescribe to patients with CKD and T2D. Finerenone is a medication that works by blocking certain proteins known as mineralocorticoid receptors. An increased stimulation of these proteins is thought to damage the kidneys and the heart. By lowering their stimulation, finerenone reduces the risk of kidney disease progressively getting worse. The main purpose of this study is to learn more about characteristics and treatment patterns of people with CKD and T2D who have recently started or will start finerenone treatment as prescribed by their doctor as part of their routine medical care in South Korea. The FINE-REAL Korea study is designed to collect additional data on people with CKD and T2D who are treated with finerenone according to the approved product information, and it will work alongside the original FINE-REAL study (NCT05348733) to gather enough information for safety assessments in Korean population. To achieve this, researchers will collect data on:

• Clinical characteristics of participants, including their medical history related to CKD and T2D, blood pressure, and heart health.
• Reasons for starting finerenone.
• Reasons for stopping finerenone early.
• The planned and actual duration of finerenone treatment.
• The dosing of finerenone.
• Other medications taken alongside finerenone. The study will also monitor any medical problems (known as adverse events) that participants may experience during the study. All adverse events will be recorded, regardless of whether they are related to the treatment. One specific concern is hyperkalemia, which refers to high potassium levels in the blood. This condition can occur when finerenone is used with certain blood pressure medications. Researchers want to understand how often hyperkalemia happens and whether it leads to:
• Early discontinuation of finerenone treatment.
• The need for dialysis, a procedure that filters waste from the blood.
• Hospitalization for care. Data for this study will be collected from medical records and through interviews conducted by study doctors during routine medical visits. Participants will be involved in the study for up to 12 months, although this duration may be shorter if their finerenone treatment is stopped early.

Conditions

Chronic Kidney Disease; Type 2 Diabetes Mellitus

Outcome Measures

Primary Outcomes (6)

• Descriptive analysis of clinical characteristics of participants with chronic kidney disease (CKD) and with type 2 diabetes (T2D)

  Up to 12 months after start of finerenone

• Descriptive summary of reasons for introducing finerenone

  Up to 12 months after start of finerenone

• Descriptive summary of reasons for discontinuation of finerenone

  Up to 12 months after start of finerenone

• Planned and actual duration of treatment with finerenone

  Up to 12 months after start of finerenone

• Planned and actual dosing of finerenone

  Up to 12 months after start of finerenone

• Descriptive summary of secondary therapies used in participants with CKD and T2D

  Up to 12 months after start of finerenone

Secondary Outcomes (2)

• Occurrence of adverse events (AEs)

  Up to 30 days after the final treatment with finerenone

• Occurrence of hyperkalemia

  Up to 30 days after the final treatment with finerenone

Study Arms (1)

Participants diagnosed with CKD and T2D

Participants who are newly prescribed finerenone under routine treatment conditions.

Drug: Kerendia (Finerenone, BAY94-8862)

Interventions

Kerendia (Finerenone, BAY94-8862) DRUG

Decision will be taken by the treating physician to initiate treatment with finerenone.

Participants diagnosed with CKD and T2D

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Participants with a diagnosed of CKD and T2D will be enrolled after the decision for treatment with finerenone has been made by the treating physician.

You may qualify if:

• Adult female or male participant - All genders (≥18 years old)
• Diagnosis of CKD associated with T2D based on assessment by physician
• Treatment according to local marketing authorization, finerenone 20 or 10 mg. Treatment should have been started up to 8 weeks before or after the ICF is signed.
• Decision to initiate treatment with finerenone must be made before ICF is signed

You may not qualify if:

• Participation in an investigational trial at any time during the course of this study
• Contra-indications according to the local label

Sponsors & Collaborators

• Bayer: lead

Study Sites (1)

Many Locations

Multiple Locations, South Korea

RECRUITING

MeSH Terms

Conditions

Renal Insufficiency, Chronic; Diabetes Mellitus, Type 2

Interventions

finerenone

Condition Hierarchy (Ancestors)

Renal Insufficiency; Kidney Diseases; Urologic Diseases; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Male Urogenital Diseases; Chronic Disease; Disease Attributes; Pathologic Processes; Pathological Conditions, Signs and Symptoms; Diabetes Mellitus; Glucose Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases

Central Study Contacts

Bayer Clinical Trials Contact

CONTACT

(+)1-888-84 22937; clinical-trials-contact@bayer.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 14, 2025
• First Posted: November 18, 2025
• Study Start: November 20, 2025
• Primary Completion (Estimated): September 30, 2027
• Study Completion (Estimated): January 28, 2028
• Last Updated: April 17, 2026

Record last verified: 2026-04

Data Sharing

• IPD Sharing: Will not share

Locations

KR (1)